Evidence map›Paper›PMID 38117375›Full record

ArticleJournal of neuro-oncology2024

Oncogene-induced senescence in meningiomas-an immunohistochemical study.

Vladimir Mijajlović, Marko Miler, Rosanda Ilić, Dejan Rašić, Duško Dunđerović, Savo Raičević, Ivan Soldatović, Silvio De Luka, Emilija Manojlović-Gačić

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Article in Journal of neuro-oncology, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing papers in PubMed
0.4field-weighted citation impact, top 31% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed, 2 citations in OpenAlex.

  1. Article
4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

9 authors at 2 institutions in 1 country.

Vladimir MijajlovićDepartment for Pathology, Pathohistology and Medical Cytology, University Clinical Centre of Serbia, Belgrade, Serbia.
Marko MilerDepartment of Cytology, Institute for Biological Research "Siniša Stanković"- National Institute of the Republic of Serbia, University of Belgrade, Belgrade, Serbia.
Rosanda IlićClinic for Neurosurgery, University Clinical Centre of Serbia, Belgrade, Serbia.
Dejan RašićClinic for Ophthalmology, University Clinical Centre of Serbia, Belgrade, Serbia.
Duško DunđerovićInstitute of Pathology, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.
Savo RaičevićDepartment for Pathology, Pathohistology and Medical Cytology, University Clinical Centre of Serbia, Belgrade, Serbia.
Ivan SoldatovićInstitute for Medical Statistics and Informatics, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.
Silvio De LukaInstitute for Pathophysiology, Faculty of Medicine, University of Belgrade, Belgrade, Serbia.
Emilija Manojlović-GačićInstitute of Pathology, Faculty of Medicine, University of Belgrade, Belgrade, Serbia. emanojlovicgacic@gmail.com.
University of Belgrade · RSUniverzitetski Klinički Centar Srbije · RS

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

purposeMeningiomas are tumours originating from meningothelial cells, the majority belonging to grade 1 according to the World Health Organization classification of the tumours of the Central Nervous System. Factors contributing to the progression to the higher grades (grades 2 and 3) have not been elucidated yet. Senescence has been proposed as a potential mechanism constraining the malignant transformation of tumours. Senescence-associated beta-galactosidase (SA-β-GAL) and inhibitors of cyclin-dependent kinases p16 and p21 have been suggested as senescence markers.

methodsWe analysed 318 meningiomas of total 343 (178 grade 1, 133 grade 2 and 7 grade 3). Tissue microarrays were constructed and stained immunohistochemically, using antibodies for SA-β-GAL, p16 and p21.

resultsThe positive correlation of the tumour grade with the expression of p16 (p = 0.016) and SA-β-GAL (p = 0.002) was observed. The expression of p16 and SA-β-GAL was significantly higher in meningiomas grade 2 compared to meningiomas grade 1 (p = 0.006 and p = 0.004, respectively). SA-β-GAL positivity positively correlated with p16 and p21 in the whole cohort. In grade 2 meningiomas, a positive correlation was only between SA-β-GAL and p16. Correlations of senescence markers in meningiomas grade 2 were not present.

conclusionOur findings suggest the senescence activation in meningiomas grade 2 as a potential mechanism for the restraining of tumour growth and give hope for applying of promising senolytic therapy.

Indexed as

Meningeal NeoplasmsMeningiomabeta-GalactosidaseCellular SenescenceCentral Nervous SystemCyclin-Dependent Kinase Inhibitor p16HumansOncogenesbeta-GalactosidaseCyclin-Dependent Kinase Inhibitor p16Atypical meningiomaBeta-galactosidaseGrade 2 meningiomap16p21Senescence

Identifiers

PMID38117375
OpenAlexW4390016168

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.